A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888318



Internal ID22663322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44626722..44626809hg38UCSC Ensembl
chr4:44628739..44628826hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421160
Samples
Known GenesYIPF7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888318
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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